Central Complex
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Central complex structure
The central
complex is a prominent protocerebral neuropil that spans over the
midline into both hemispheres. Its main component is the central
body with an upper and lower division. The division are joined by
two small neuropils structures, the noduli. The central complex
includes another mid-line neuropil structure, the protocerebral
bridge. In Diptera (such as the fruit fly), the upper division is
called fan-shaped body and the lower division ellipsoid
body(Hanesch
et al., 1989; Young et al., 2009).
Properties of the central
complex
Polarisation sensitivity
In the
locust, about 20% of the central complex neurons have beens shown
to display polarisation sensitive responses to light. In particular
neurons of the lower division of the central body show polarisation
sensitivity. The lower division appears to be less developed in
insects that do not have polarisation vision.
Role
in visual learning
In the fruit fly, it has been suggested
that the central body is involved in visual learning, in
particular, the fan-shaped body is thought to be important for
learning spatial patterns of visual stimuli [Liu et al., 2006].In
navigation tasks with visual cues, the ellipsoid body appears to be
important [Neuser et al., 2008].
Generation
of courtship song
Block of neurotransmission though
acetylcholine or NO in the central body leads to impairments of
courtship song generation in crickets. Thus, the central body is
implied to be a crucial element in the generation of the courtship
song pattern [Hoffmann et al., 2007; Weinrich et al.,
2008].
Integrative
properties
Many neurons of the central complex are
multimodal and can display complex event-related activities
[Homberg 1985; 1994].The
central complex can thus be viewed as an important structure for
the integration of information in the insect brain.
Dispositions
of central complex neurons
The cytoarchitecture of
the central complex has been most intensively studied in flies (in
particular Drosophila) and in locusts (Locusta, Schistocerca).
Tangential cells
Tangential neurons are the
primary input neurons of the central complex. The innervate various
areas of the adjacent protocerebrum including the posterior optic
tubercle and lateral accessory lobe and many, if not all columns of
the central body or subdivisions of the protocerebral bridge.
Columnar cells
Columnar cells are the main output
elements of the central body and their morphology can be used to
divide the central body into distict columns innervated by these
neurons. The columnar cells make topographically arranged
connections between the left and right sides of the central body.
Projection targets are the noduli and the lateral accessory lobes.
Pontine cells
Pontine cells make topographically
arranged connections between the left and right sides of the upper
division of the central body, in some cases in different layers.
References
Hanesch U, Fischbach KF, Heisenberg M (1989) Neuronal
architecture of the central complex in Drosophila melanogaster.
Cell Tissue Res 257:343-366.
Homberg U (1994)
Flight-correlated activity changes in neurons of the lateral
accessory lobes in the brain of the locust Schistocerca gregaria. J
Comp Physiol A 175:597-610.
Liu G, Seiler H, When A, Zars T,
Ito K, Wolf R, Heisenberg M, Liu L (2006) Distinct memory traces
for two visual features in the Drosophila brain. Nature
439:551-556.
Neuser K, Triphan T, Mronz M, Poeck B, Strauss
R (2008) Analysis of a spatial orientation memory in Drosophila.
Nature 453:1244-1247.
Weinrich A, Kunst M, Wirmer A,
Holstein GR, Heinrich R (2008) Suppression of grasshopper sound
production by nitric oxide-releasing neurons of the central
complex. J Comp Physiol A 194:763-776.
Young JM, Armstrong
JD (2009) Structure of the adult central complex in Drosophila:
Organization of distinct neuronal subsets. J Comp Neurol
518:1500-1524.